Clinical Protocol Jobs

Telix Pharmaceuticals is hiring a seasoned Medical Writer to lead and produce regulatory and clinical documentation for global submissions supporting its oncology and rare‑disease radiopharmaceutical portfolio.

Experienced physician-scientist needed to drive clinical trial design and medical oversight for prostate and renal oncology programs at Regeneron.

ORIC Pharmaceuticals is hiring a Senior Clinical Trial Manager to lead global oncology trials, manage vendors/CROs, and drive study execution from start-up through database lock in a hybrid San Diego role.

AbbVie is hiring a Study Project Manager II to lead end-to-end clinical study operations, drive strategic planning and execution, and ensure compliant, timely delivery across study phases.

Bristol Myers Squibb seeks a Clinical Scientist in Hematology to design and execute assigned clinical trial activities and contribute medical and scientific input across study deliverables.

Experienced Clinical Research Coordinator needed to lead and coordinate vaccine trial activities onsite at a Profound Research community site in Oceanside, CA.

Exact Sciences is hiring an Associate Director of Clinical Operations to lead a Clinical Affairs team and drive end-to-end execution of clinical studies supporting diagnostic development.

AbbVie is hiring a Study Project Manager I to lead cross-functional clinical study teams and drive operational excellence across study planning, execution and vendor management.

Experienced clinical research coordinator needed to manage and execute complex neuro-oncology therapeutic interventional trials at OHSU’s Knight Cancer Institute, ensuring patient safety, regulatory compliance, and accurate trial documentation.

Senior clinical leader needed to drive obesity and endocrinology clinical development programs, mentor teams, and represent AbbVie in cross-functional and regulatory settings.

Rho is hiring a board-certified Psychiatrist to serve as a remote Medical Director responsible for medical monitoring, safety review, and clinical development input across global clinical trial programs.

Northwestern Medicine seeks a Senior Regulatory Coordinator to lead IRB submissions and regulatory oversight for complex stem cell transplant and cell therapy studies within the Autoimmune Diseases program.

Clinical Research Coordinator A/B needed at Penn's CCI to support coordination, documentation, and regulatory compliance for early-phase oncology cell and gene therapy trials.

Experienced physician needed to serve as Medical Director at a collaborative CRO, providing medical oversight, safety review, and scientific guidance across clinical programs.

Care Access Research is hiring a Source Document Specialist to design, maintain, and version-control compliant eSource and paper source documents for remote clinical trial operations.

Experienced MD clinical leader sought to lead and execute global renal development programs, owning benefit-risk assessment and regulatory-ready clinical strategy.

Care Access seeks an experienced Travel Clinical Research Coordinator based in Dallas to manage and execute multi-site clinical trial activities while traveling up to 75% nationwide.

Experienced vaccines clinical scientist to lead program-level clinical design, scientific oversight, and cross-functional execution for global studies at Pfizer.

St. Jude Children's Research Hospital seeks a Clinical Research Scientist I in Epidemiology and Cancer Control to lead study design, coordinate multi-site research operations, and advance population-based cancer outcomes research.

Senior medical affairs leader needed to drive oncology/hematology strategy, clinical evidence generation, and cross-functional medical support for AbbVie's product portfolio in a hybrid San Francisco role.

Emory University is hiring a Regulatory Specialist II to manage IRB submissions, regulatory compliance, and trial documentation for a portfolio of clinical studies with hybrid work flexibility.

Experienced medical leader needed to drive US medical strategy, clinical development, and stakeholder engagement for Novartis cardiovascular programs in a remote capacity across the United States.

A two-year onsite rotational program at AbbVie’s North Chicago HQ that develops specialist physicians into Associate Medical Directors through cross-functional R&D rotations in oncology and related therapeutic areas.

AbbVie seeks an experienced Medical Director in Clinical Development (Neuroscience) to lead complex clinical programs, shape development strategy, and ensure high-quality clinical data and regulatory readiness.

Experienced oncology medical affairs leader needed to drive scientific strategy, clinical evidence generation, medical education, and safety oversight for AbbVie’s hematology/oncology programs on a hybrid schedule based in Mettawa, IL.

AbbVie seeks M.D./D.O. candidates (recent residency or fellowship graduates) for a two-year, onsite Physician Development Program in Neuroscience and related therapeutic areas, entering as Associate Medical Directors to gain cross-functional R&D experience.

Senior medical writer and team lead role responsible for authoring regulatory submissions and maturing medical writing processes at a growth-stage biotech focused on immunology.

AbbVie is hiring Associate Medical Directors for a two-year onsite Physician’s Development Program in North Chicago, focused on developing fellows into R&D medical leaders across clinical development, safety, regulatory, and medical affairs.